| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g47600 | A09 | 51807751 | C | T | missense_variant | MODERATE | c.803G>A|p.Arg268Lys |
S30 S31 |
| 2 | BAA09g47600 | A09 | 51811227 | G | A | upstream_gene_variant | MODIFIER | c.-1994C>T| |
S34 |
| 3 | BAA09g47600 | A09 | 51812578 | G | A | upstream_gene_variant | MODIFIER | c.-3345C>T| |
S69 |
| 4 | BAA09g47600 | A09 | 51812684 | T | A | upstream_gene_variant | MODIFIER | c.-3451A>T| |
S65 |
| 5 | BAA09g47600 | A09 | 51812778 | C | T | upstream_gene_variant | MODIFIER | c.-3545G>A| |
S188 S276 |
| 6 | BAA09g47600 | A09 | 51813004 | C | T | upstream_gene_variant | MODIFIER | c.-3771G>A| |
S259 |
| 7 | BAA09g47600 | A09 | 51813060 | C | T | upstream_gene_variant | MODIFIER | c.-3827G>A| |
S208 |
| 8 | BAA09g47600 | A09 | 51814160 | G | A | upstream_gene_variant | MODIFIER | c.-4927C>T| |
S218 |